OTAK:AM Capsules recalled for undeclared milk allergen
NutraCap Labs LLC is recalling OTAK Innovations OTAK:AM Capsules 90ct bottles due to undeclared milk content. The product was distributed across 25 states.
The agency’s classification
FDA (Food): Class I
Class I is a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 4/5 (Severe).
The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The FDA classified this as Class I. Per the rubric, FDA Class I recalls without reported deaths merit a score of 4 (Severe), as they present a serious risk to health. Undeclared milk allergen poses significant risk to allergic individuals.
Plain-English summary
NutraCap Labs LLC is recalling OTAK Innovations OTAK:AM Capsules 90ct Bottle (UPC 4 08012 0204) because the product contains undeclared milk. During an FDA investigation, the firm was notified of the undeclared allergen.
Approximately 80,169 various bottles and jars were distributed to consumers in the following states: Alabama, Arkansas, Arizona, California, Colorado, Connecticut, Florida, Georgia, Idaho, Illinois, Indiana, Kentucky, Louisiana, Maryland, Minnesota, North Carolina, New Jersey, Nevada, New York, Ohio, Oregon, South Carolina, Tennessee, Texas, Virginia, and Washington.
The affected product has Lot #2007073 with an expiration date of 07/2022. Consumers who have purchased this product and have a milk allergy or sensitivity should stop using it and consult their healthcare provider if they have consumed the product.
The recalled product
- Product
- OTAK Innovations OTAK:AM Capsules 90ct Bottle UPC CODE 4 08012 0204
- Manufacturer
- NutraCap Labs LLC
- Category
- Food — Dietary Supplement
- Affected units
- 80,169
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- LOT #2007073 EXP DATE 07/2022
Distribution
Part of a larger recall action
This product is one of 106 recalled by NutraCap Labs LLC under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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